• Keine Ergebnisse gefunden

Quantized thermal transport in single-atom junctions

N/A
N/A
Protected

Academic year: 2022

Aktie "Quantized thermal transport in single-atom junctions"

Copied!
4
0
0

Wird geladen.... (Jetzt Volltext ansehen)

Volltext

(1)

Quantized thermal transport in single-atom junctions

Longji Cui,1*Wonho Jeong,1*Sunghoon Hur,1Manuel Matt,2Jan C. Klöckner,2 Fabian Pauly,2Peter Nielaba,2Juan Carlos Cuevas,3

Edgar Meyhofer,1†Pramod Reddy1,4

Thermal transport in individual atomic junctions and chains is of great fundamental interest because of the distinctive quantum effects expected to arise in them.

By using novel, custom-fabricated, picowatt-resolution calorimetric scanning probes, we measured the thermal conductance of gold and platinum metallic wires down to single- atom junctions. Our work reveals that the thermal conductance of gold single-atom junctions is quantized at room temperature and shows that the Wiedemann-Franz law relating thermal and electrical conductance is satisfied even in single-atom contacts.

Furthermore, we quantitatively explain our experimental results within the Landauer framework for quantum thermal transport. The experimental techniques reported here will enable thermal transport studies in atomic and molecular chains, which will be key to investigating numerous fundamental issues that thus far have remained experimentally inaccessible.

T

he study of thermal transport at the nano- scale is of critical importance for the devel- opment of novel nanoelectronic devices and holds promise to unravel quantum phenome- na that have no classical analogs (1–3). In the context of nanoscale devices, metallic atomic-size contacts (4) and single-molecule junctions (5) rep- resent the ultimate limit of miniaturization and have emerged as paradigmatic systems revealing previously unknown quantum effects related to charge and energy transport. For instance, trans- port properties of atomic-scale systems—such as electrical conductance (6), shot noise (7,8), thermo- power (9–11), and Joule heating (12)—are completely dominated by quantum effects, even at room temperature. Therefore, they drastically differ from those of macroscale devices. Unfortunately, the experimental study of thermal transport in these systems constitutes a formidable challenge and has remained elusive to date, in spite of its fun- damental interest (13).

Probing thermal transport in junctions of atom- ic dimensions is crucial for understanding the ul- timate quantum limits of energy transport. These limits have been explored in a variety of micro- devices (14–18), where it has been shown that, irrespective of the nature of the carriers (pho- nons, photons, or electrons), heat is ultimately transported via discrete channels. The maximum

contribution per channel to the thermal conduct- ance is equal to the universal thermal conduct- ance quantumG0,Th=p2kB2T/3h, wherekBis the Boltzmann constant,Tis the absolute temper- ature, andhis the Planck’s constant. However, observations of quantum thermal transport in microscale devices have only been possible at sub-Kelvin temperatures, and other attempts at higher-temperature regimes have yielded incon- clusive results (19).

The energy-level spacing in metallic contacts of atomic size is of the order of electron volts (i.e., much larger than thermal energy); therefore, these junctions offer an opportunity to explore whether thermal transport can still be quantized at room temperature. However, probing thermal transport in atomic junctions is challenging because of the technical obstacles in reproducibly creating stable atomic junctions while measuring the miniscule heat currents flowing through the atomic chains.

We present an experimental platform that allows us to measure the thermal conductance of metal- lic wires down to the single-atom limit. With this technique, we were able to observe quantized thermal transport at room temperature. Spe- cifically, we developed an approach that uses custom-fabricated calorimetric scanning thermal microscopy (C-SThM; Fig. 1) probes, which feature a very large thermal resistance (RP≈1.3 × 106K/W) and high-resolution Pt thermometers with a tem- perature resolution (DTmin) of ~0.6 mK in a 10-Hz bandwidth (20–22). These characteristics enable thermal conductance measurements with ~25-pW/K resolution when a temperature bias of ~20 K is applied across atomic junctions. We achieved the large thermal resistance by incorporating long, T-shaped beams with a small cross-sectional area, which also enable a very high stiffness (>104N/m in the normal direction) (20). Both of these fea-

tures are critical for accomplishing atomic junc- tion thermal measurements. The C-SThM probes also have a sharp metallic tip that we coated with Au or Pt, but which can also be coated with other metals (20).

Our strategy for quantitatively measuring the thermal conductance of atomic junctions is de- picted in Fig. 1A. We heated the Au substrate to a temperatureTS= 315 K while the probe was connected to a thermal reservoir atT0= 295 K.

We then displaced the probe toward the heated substrate by piezoelectric actuation until we reached an electrical conductance of 4G0, with G0= 2e2/h≈(12.9 kiloohm)1being the elec- trical conductance quantum. This electrical con- ductance signals the formation of a Au-Au contact involving several atoms, as established by past work (4). We measured the probe-substrate elec- trical conductance by applying a small sinusoidal voltage bias with an amplitude of 1 mV at a fre- quency of 10 kHz and recording the amplitude of the resultant electric current with a lock-in amplifier (20). Once we reached the threshold conductance, we withdrew the probe slowly from the substrate at a rate of 0.05 nm/s. During this process, the probe-substrate contact region is ex- pected to become more constricted until it forms a single-atom-wide junction, which is broken upon further withdrawal (Fig. 1B) (23). We concurrently performed thermal conductance measurements by continuously measuring the change in probe tem- perature (DTP) in response to heat flow (Q) through the atomic junction. We measured the probe tem- perature by monitoring the change in the resist- ance of the embedded Pt resistance thermometer via a sinusoidal electrical current of fixed ampli- tude (10mA) and frequency (1 kHz) supplied to the probe, while measuring the voltage drop across the resistor.

From the resistance network (Fig. 1A), we directly related the thermal conductance (GTh) of the atomic junctions toDTPbyGTh=DTP/[RP(TS–T0–DTP)], whereRPwas 1.3 × 106K/W (20). Representa- tive thermal (red) and electrical conductance (blue) traces show that the electrical conductance de- creases in discrete steps (Fig. 2A). Many of the curves exhibit preferential conductance values that occur at integer multiples ofG0, as expected from past work (4). The corresponding thermal conductance curves closely correlate to the elec- trical conductance curves. Further, several of the thermal conductance curves show steps with pre- ferential conductances at 2p2kB

2T/3h, a value that is twice the quantum of thermal conductance (G0,Th). The factor of 2 is a consequence of the spin degeneracy in electron transport and is not present in the usual definition ofG0,Thbecause it was introduced in the context of phonon trans- port, where spin degeneracy is absent.

Past studies (24–26) on electrical conduct- ance quantization established that the presence of plateaus in the conductance traces is insuffi- cient evidence of quantization. Definitive conduct- ance quantization requires an unbiased statistical analysis from a large data set. We obtained ~2000 consecutive electrical and thermal conductance traces with the procedure outlined above, which

1

1Department of Mechanical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.2Department of Physics, University of Konstanz, D-78457 Konstanz, Germany.3Departamento de Física Teórica de la Materia Condensada and Condensed Matter Physics Center (IFIMAC), Universidad Autónoma de Madrid, Madrid 28049, Spain.4Department of Materials Science and Engineering, University of Michigan, Ann Arbor, MI 48109, USA.

*These authors contributed equally to this work.†Corresponding author. Email: juancarlos.cuevas@uam.es (J.C.C.); meyhofer@

umich.edu (E.M.); pramodr@umich.edu (P.R.)

Konstanzer Online-Publikations-System (KOPS) URL: http://nbn-resolving.de/urn:nbn:de:bsz:352-0-399840

Erschienen in: Science ; 355 (2017), 6330. - S. 1192-1195 https://dx.doi.org/10.1126/science.aam6622

(2)

Fig. 1. Experimental setup and scanning electron microscopy (SEM) images of the scanning ther- mal probes.(A) Schematic of a calorimetric scan- ning thermal microscopy (C-SThM) probe, which is used to make atomic junctions with a heated me- tallic substrate. The tip and substrate coatings can be either Au or Pt. The electrical conductance of the tip-substrate junction is monitored by applying a small sinusoidal voltage bias and measuring the resultant current. The resistance of the Pt resistance thermom- eter is monitored by applying a sinusoidal current (amplitude If) and recording the voltage output (Vf). A thermal resistance network describes the resistances of the atomic chain [RAtom= (GTh)−1] and the scanning probe (RP), as well as the heat current flow (Q, red arrow). The substrate, thermal reservoir, and tip temperatures are indicated by TS,T0, andTP, respectively. (B) Schematics of the atomic chains forming, narrowing, and breaking during the withdrawal of the probe from the heated substrate.

(C) SEM image (side view) of a scanning probe with two long and stiff T-shaped SiNxbeams. (D) SEM image (top view) of the scanning probe, featuring a Au-coated tip (inset) and a serpentine Pt thermometer.

Fig. 2. Thermal conductance quantization in Au atomic junctions.(A) Representative traces of ther- mal and electrical conductances measured while reducing the transverse constriction of Au atomic junctions by displacing the Au tip of the C-SThM probe away from the Au substrate. The thermal (red) and electrical (blue) conductance traces are plotted in units of 2π2kB2T/3h(2G0,Th, twice the thermal conductance quantum) and 2e2/h(G0, the electrical conductance quantum), respectively.

(B) Histogram of the ratio of the thermal conduct- ance to the electrical conductance, showing good agreement with the Lorenz number (L/L0). The color bar indicates the number of counts, increasing from white to red. (CandD) Electrical and thermal con- ductance histograms obtained from 2000 concur- rently measured electrical and thermal conductance traces (without any data selection), similar to those shown in (A). (E) A joint plot of the electrical and thermal conductance traces shows the tight corre- lation between the occurrence of electrical and ther- mal conductance quantization. (F) Analysis of the data in (C) and (D) shows that the Wiedemann- Franz law accurately predicts the thermal conduct- ance of Au atomic junctions (the peak is at 1.06). a.u., arbitrary units.

2

(3)

yielded electrical and thermal conductance histo- grams with clear peaks at 1G0and 2G0,Th, respec- tively (Fig. 2, C and D). The thermal conductance histogram is broader than its electrical counter- part because the time constant for our thermal measurements (~25 ms) (20) is larger than that for our electrical measurements (~10ms).

The close correlation between the thermal and electrical conductances (Fig. 2A) provides important information regarding the validity of the Wiedemann-Franz law, which relates the electronic contribution of the thermal conduct- ance,GTh,e, to the electrical conductance,Ge, by GTh,e =L0TGe, whereL0= (p2/3)(kB/e)2is the Lorenz number (27). Because this basic law was originally derived with semiclassical arguments and is approximately obeyed in macroscopic wires of standard metals (27), it is unclear whether it should remain valid in metallic atomic junctions, where the transport mechanisms are different (28). To test the validity of the Wiedemann-Franz law in atomic junctions, we used the data in Fig.

2A to obtain the Lorenz ratio,L/L0=GTh/L0GeT, as a function ofGe. Here,T= 305 K is the av-

erage temperature of the tip and the sample. This process was repeated for each set of curves shown in Fig. 2A, and the data from all four curves were collected into the two-dimensional (2D) histogram shown in Fig. 2B (20). It is clear from the data that the value ofL/L0is very close to 1.

We plotted a 3D histogram from 2000 concur- rently measured electrical and thermal conduct- ance traces, without any data selection (Fig. 2E) (20). The histogram features a large peak corre- sponding to (G0, 2G0,Th), showing that the elec- trical and thermal conductance quantization occurs concurrently and that the quantized state is a sta- tistically favored atomic configuration. This close correlation is also reflected in the 2D histogram (Fig. 2F), where we computedL/L0=GTh/L0GeT= 1.06 as mean value from the 2000 traces (20). The small increase above 1.00 is primarily due to con- tributions from phonons to the thermal conduct- ance, which we estimate to add ~5 to 10% (see below). The increase inL/L0could also reflect small contributions (~10 to 20 pW/K) from near- field radiative heat transfer (29) and even smaller contributions from the overestimation of the ther-

mal conductance during periods of rapid tran- sition in the electrical conductance, when the thermal response lags the electrical response.

To unambiguously identify the origin of our quantization observations, we used custom- developed methods to compute the thermal and electrical conductance of Au atomic-size contacts within the framework of the Landauer-Büttiker formalism for coherent transport. We exactly simulated the experiments by using a combina- tion of molecular dynamics (MD) (11, 30, 31), density functional theory (DFT) (32,33), and nonequilibrium Green’s function techniques to describe the contributions of both electrons and phonons to the thermal conductance (20).

Our MD simulations (movies S1 to S6) show that when the electrical conductance is G0,the atomic junction typically has an atomic“dimer” bridge geometry, similar to that shown in the inset of Fig. 3A. Our DFT-based calculations (Fig. 3A) for the electrical and thermal trans- port for a dimer geometry show that the thermal conductance at room temperature is dominated by the electronic contribution, with phonons giv- ing only ~4% of the total signal, which is similar to the case of bulk Au wires (34). We also found that the electronic contribution at room temper- ature in this example isGTh,e≈0.59 nW/K, which is close to twice the thermal conductance quan- tum. The reason for this quantized thermal con- ductance is apparent from Fig. 3B, where we show that electronic transmission is dominated by a single (spin-degenerate) conduction channel and has a value very close to 1. This fact, taken together with the smooth energy dependence of the electronic transmission around the Fermi energy (20), leads to excellent agreement with the Wiedemann-Franz law:GTh,e≈L0TGe≈2G0,Th. Therefore, we conclude that for one-atom Au junctions, the observed thermal conductance quantization is intricately linked to the electronic structure of this monovalent metal.

Having established the origin of thermal con- ductance quantization and the small contribu- tion of phonons, we focused on the analysis of GTh,eto systematically study the validity of the Wiedemann-Franz law for Au contacts of arbitrary size. For this purpose, we performed 100 simu- lations of the formation of Au junctions at 300 K while computing the electrical and thermal con- ductance for the transient geometries. We present histograms constructed from the electrical and thermal conductance traces (Fig. 3C). The elec- trical conductance histogram is dominated by a peak close to 1G0, which is due to preferen- tial formation of one-atom-thick contacts and short atomic chains (11). The corresponding histo- gram for the thermal conductance (normalized by 2G0,Th) shows a very close correlation with the electrical one. Therefore, the Wiedemann-Franz law,GTh,e≈ L0TGe, holds almost exactly, irre- spective of the electrical conductance value (i.e., contact size) (Fig. 3D). Although some fine details of the experimental histograms are not reproduced, these computational results are in excellent agree- ment with our experiments (Fig. 2) and provide compelling evidence that the quantized thermal

3 Fig. 3. Computations of thermal conductance in Au atomic junctions.(A) Computed thermal

conductance as a function of temperature for the Au atomic junction geometry shown in the inset. The total thermal conductanceGTh,total(black), the electronic contributionGTh,e(blue), and the phononic contribution GTh,ph(red) to thermal conductance are shown.GTh,phis almost negligible at room temperature. (B) The total electronic transmissionttotaland the individual electronic transmission coefficientst1tot4, as a function of the energy (measured with respect to the Fermi energyEF) for the contact geometry in the inset of (A). The electronic transmission is dominated by a single (spin-degenerate) conduction channel. (C) Electrical and electronic thermal conductance histograms obtained from 100 MD simulations of the formation of Au atomic contacts at room temperature (insets show representative electrical and thermal conductance traces obtained from these simulations). (D) Lorenz ratio (L/L0) as a function of the electrical conductanceGeof the Au contacts, as obtained from the histograms in (C). The ratio is very close to 1. Deviations are below 1%, which shows that the Wiedemann-Franz law is fulfilled with good accuracy, irrespective of the contact size.

(4)

transport that we observed corresponds to Au single-atom junctions and is not affected by sur- face contaminants, which are known to plague nano-gap thermal transport measurements (29).

The observed thermal conductance quantiza- tion in Au junctions is a direct consequence of the electronic structure of these junctions, which in turn is also responsible for the validity of the Wiedemann-Franz law. However, the opposite is not true: The validity of the Wiedemann-Franz law is a consequence of the smooth energy dependence of the electronic transmission (35,36), but this does not imply that thermal transport is quantized in all cases. For example, our simulations of the Pt atom- ic junctions suggest that although the electrical and thermal conductance traces show discrete steps and are in agreement with the Wiedemann-Franz law (Fig. 4A), one should not expect electrical or thermal conductance quantization (20). Even a single-atom contact of Pt sustains multiple con- duction channels with intermediate transmissions between 0 and 1 that contribute to the transport properties (Fig. 4B), which is at variance with the Au case. These additional channels originate from the contribution of d-orbitals in Pt (11). Further, our simulations show that the electrical and ther- mal conductance histograms for Pt are relatively

featureless and that there are no strongly preferred conductance values at room temperature (20).

To unambiguously test these predictions, we performed measurements with a Pt-coated scann- ing probe and a Pt substrate, using the same meth- odology that we used for Au atom junctions. The measured electrical and thermal conductance traces (Fig. 4C) show plateaus. A histogram-based analysis of 100 Pt traces (Fig. 4D) revealed that the Lorenz ratio is very close to 1 and therefore obeys the Wiedemann-Franz law. However, histograms of electrical and thermal conductance traces do not show conductance quantization (20), in agreement with our computational predictions. This demon- strates that thermal conductance quantization is not a universal feature of all metallic systems at room temperature.

Our work provides insights into thermal trans- port in atomic-size Au and Pt contacts and reveals conductance quantization at room temperature in Au atom junctions. We have also established the ap- plicability of the Wiedemann-Franz law for analyz- ing thermal transport in metallic atomic-size contacts.

The scanning calorimetric probes described here will enable thermal transport studies in molecular junctions, 1D chains of atoms, and individual pol- ymer chains, all of which have been studied theo-

retically and computationally for more than half a century (13,37) but have not been probed experi- mentally because of the lack of experimental tools.

R E F E R E N C E S A N D N OT E S 1. E. Pop,Nano Res.3, 147–169 (2010).

2. D. G. Cahillet al.,Appl. Phys. Rev.1, 011305 (2014).

3. J. Crossnoet al.,Science351, 1058–1061 (2016).

4. N. Agraït, A. L. Yeyati, J. M. van Ruitenbeek,Phys. Rep.377, 81–279 (2003).

5. J. C. Cuevas, E. Scheer,Molecular Electronics: An Introduction to Theory and Experiment(World Scientific Series in Nanoscience and Nanotechnology, World Scientific, 2010).

6. E. Scheeret al.,Nature394, 154–157 (1998).

7. H. E. van den Brom, J. M. van Ruitenbeek,Phys. Rev. Lett.82, 1526–1529 (1999).

8. P. J. Wheeler, J. N. Russom, K. Evans, N. S. King, D. Natelson, Nano Lett.10, 1287–1292 (2010).

9. B. Ludoph, J. M. van Ruitenbeek,Phys. Rev. B59, 12290–12293 (1999).

10. P. Reddy, S. Y. Jang, R. A. Segalman, A. Majumdar,Science 315, 1568–1571 (2007).

11. C. Evangeliet al.,Nano Lett.15, 1006–1011 (2015).

12. W. Leeet al.,Nature498, 209–212 (2013).

13. Y. Dubi, M. Di Ventra,Rev. Mod. Phys.83, 131–155 (2011).

14. K. Schwab, E. A. Henriksen, J. M. Worlock, M. L. Roukes,Nature 404, 974–977 (2000).

15. O. Chiattiet al.,Phys. Rev. Lett.97, 056601 (2006).

16. M. Meschke, W. Guichard, J. P. Pekola,Nature444, 187–190 (2006).

17. S. Jezouinet al.,Science342, 601–604 (2013).

18. M. Partanenet al.,Nat. Phys.12, 460–464 (2016).

19. B. Gotsmann, M. A. Lantz,Nat. Mater.12, 59–65 (2013).

20. Materials and methods are available as supplementary materials.

21. S. Sadat, E. Meyhofer, P. Reddy,Rev. Sci. Instrum.83, 084902 (2012).

22. S. Sadat, E. Meyhofer, P. Reddy,Appl. Phys. Lett.102, 163110 (2013).

23. B. Xu, N. J. Tao,Science301, 1221–1223 (2003).

24. L. Olesenet al.,Phys. Rev. Lett.72, 2251–2254 (1994).

25. J. M. Kranset al.,Phys. Rev. Lett.74, 2146 (1995).

26. L. Olesenet al.,Phys. Rev. Lett.74, 2147 (1995).

27. N. W. Ashcroft, N. D. Mermin,Solid State Physics(Holt, 1976).

28. U. Sivan, Y. Imry,Phys. Rev. B33, 551–558 (1986).

29. L. Cuiet al.,Nat. Commun.8, 14479 (2017).

30. M. Dreheret al.,Phys. Rev. B72, 075435 (2005).

31. C. Schirmet al.,Nat. Nanotechnol.8, 645–648 (2013).

32. F. Paulyet al.,New J. Phys.10, 125019 (2008).

33. M. Bürkle, T. J. Hellmuth, F. Pauly, Y. Asai,Phys. Rev. B91, 165419 (2015).

34. A. Jain, A. J. H. McGaughey,Phys. Rev. B93, 081206 (2016).

35. J. P. Bergfield, C. A. Stafford,Nano Lett.9, 3072–3076 (2009).

36. V. Balachandran, R. Bosisio, G. Benenti,Phys. Rev. B86, 035433 (2012).

37. N. Liet al.,Rev. Mod. Phys.84, 1045–1066 (2012).

AC K NOW L E D GM E NTS

P.R. acknowledges support from the U.S. Department of Energy Basic Energy Sciences program (award no. DE-SC0004871). P.R.

and E.M. acknowledge support from the U.S. Office of Naval Research (N00014-16-1-2672) and the U.S. National Science Foundation (CBET 1235691). J.C.C. acknowledges funding from the Spanish Ministry of Economy, Industry and Competitiveness (contract no. FIS2014-53488-P) and thanks the German Research Foundation (DFG) and Collaborative Research Center (SFB) 767 for sponsoring his stay at the University of Konstanz as a Mercator Fellow. M.M. and P.N. acknowledge funding from the SFB 767 and computer time granted by the John von Neumann Institute for Computing and the bwHPC framework program of the State of Baden-Württemberg, Germany. J.C.K. and F.P. were financially supported by the Carl Zeiss Foundation, the SFB 767 of the DFG, and the Junior Professorship Program of the Baden-Württemberg Ministry of Science, Research, and the Arts. We acknowledge the Lurie Nanofabrication Facility for facilitating the fabrication of devices. All of the data are available in the main paper and the supplementary materials.

4 Fig. 4. Calculated and measured transport properties of Pt atomic junctions.(A) Representative

traces of the electrical conductance (blue) and the electronic thermal conductance (red) for Pt junctions, calculated by combined MD and transport simulations. (B) The total electronic transmission and the individual electronic transmission coefficients as a function of the energy (measured with respect to the Fermi energy EF) for the contact geometry shown in the inset. The electronic transmission has substantive contributions from three channels at the Fermi level. In addition, the transmission varies more rapidly with energy than for Au atomic junctions. (C) Representative measured traces of electrical (blue) and thermal (red) conductances for Pt atomic junctions show discrete steps (conductance histograms do not display electrical or thermal conductance quantization) (20). (D) Histogram similar to that shown in Fig. 2F but for Pt data, showing that the Wiedemann-Franz law is applicable (the peak is at 1.04). The corresponding theoretical results can be seen in fig. S10 (20).

Referenzen

ÄHNLICHE DOKUMENTE

2 Here, primarily the results of the Au-Au contacts are discussed, since in this work the same kind of contact was used... For large contacts the thermovoltage reaches the positive

As a first step we have determined the preferred con- ductance values of few-atom contacts when opening or closing continuously and have constructed the corre- sponding

Our analysis of the conduction channels shows that the conductance is dominated by a single channel in the last plateau, which corresponds to a single-atom contact or a chain of

It is thus possible to investigate impor- tant properties like the superconducting density of states for metals for which the standard fabrication methods of tunnel contacts do not

We report a new analysis of shot noise over entire ensembles of junction configurations using scanning tunneling microscope-style gold break junctions at room temperature in

We find signs of non-negligible conduction from additional quantum channels in the nominal tunneling region, and observe minima in the shot noise variance coincident with

With the aim of clarifying the transport properties of single AzoTM molecules, the I-V characteristics were mea- sured at the lowest conductance regime for cis and trans isomers

A possible interpretation is that the signal for the electrolytic cell in Figure 2a does not originate from the nanoscopic ohmic contact between the two working electrodes (formed by